Biochemical fingerprints of prion diseases: Scrapie prion protein in human prion diseases that share prion genotype and type

Journal of Neurochemistry

Volumn 92, Issue 1, 2005, Pages 132-142

  Pan, Tao ^a   Li, Ruliang ^a   Kang, Shin Chung ^a   Pastore, Manuela ^a   Wong, Boon Seng ^b   Ironside, James ^b   Gambetti, Pierluigi ^a   Sy, Man Sun ^c  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

2 D electrophoresis; Prion CJD; sCJD; vCJD

Indexed keywords

GLYCAN; PRION PROTEIN; SCRAPIE PRION PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; CELL HETEROGENEITY; CODON USAGE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; FATAL FAMILIAL INSOMNIA; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN TISSUE; IMMUNOBLOTTING; PRION DISEASE; PRIORITY JOURNAL; TWO DIMENSIONAL GEL ELECTROPHORESIS;

BIOLOGICAL MARKERS; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; GENOTYPE; HUMANS; PEPTIDE MAPPING; PRION DISEASES; PRPSC PROTEINS;

SCRAPIE PRION;

EID: 13244273868     PISSN: 00223042     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1471-4159.2004.02859.x     Document Type: Article

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